Corlanor Case Study

1185 Words3 Pages

During my institutional rotation at Mount Sinai St. Lukes, I was asked a drug information question on what is Corlanor (ivabradine) and whether heart failure patents would benefit from using this drug.
Corlanor use is indicated to reduce the risk of hospitalization for worsening heart failure in patients with stable, symptomatic chronic heart failure with left ventricular ejection fraction ≤ 35%, who are in sinus rhythm with resting heart rate ≥ 70 beats per minute and either are on maximally tolerated doses of betablockers or have a contraindication to beta-blocker use. The recommended starting dose of Corlanor is 5 mg twice daily with meals. Assess patients after two weeks and adjust dose to achieve a resting heart rate between 50 and 60 beats per minute. Thereafter, adjust dose as needed based on resting heart rate and tolerability. The maximum dose is 7.5 mg twice daily. In patients with a history of conduction defects, or other patients in whom bradycardia could lead to hemodynamic compromise, initiate therapy at …show more content…

The tablet is scored and can be divided into equal halves to provide a 2.5 mg dose. Corlanor 7.5 mg: salmon-colored, triangular-shaped, film-coated tablet debossed with “7.5” on one face and plain on the other face.
Cornlanor has a contraindication to patients with acute decompensated heart failure, blood pressure less than 90/50 mmHg, sick sinus syndrome, sinoatrial block, or 3rd degree AV block, unless a functioning demand pacemaker is present, resting heart rate less than 60 bpm prior to treatment, severe hepatic impairment, pacemaker dependence (heart rate maintained exclusively by the pacemaker), concomitant use of strong cytochrome P450 3A4 (CYP3A4) inhibitors. Some common side effects include: Bradycardia, atrial fibrillation, bradyarryhthymias, hypertension, and visual brightness due to

More about Corlanor Case Study

Open Document